• 1. Catalyst-free chemoselective α-sulfenylation/β-thiolation for α,β-unsaturated carbonyl compounds
  Xi Huang,Juan Li,Xiang Li,Jiayi Wang,Yanqing Peng,Gonghua Song RSC Adv. 2019 9 26419
• 2. Catalyst-free chemoselective α-sulfenylation/β-thiolation for α,β-unsaturated carbonyl compounds
  Xi Huang,Juan Li,Xiang Li,Jiayi Wang,Yanqing Peng,Gonghua Song RSC Adv. 2019 9 26419
• 3. Catalytic enantioselective α-sulfenylation of β-ketocarbonyls by chiral primary amines
  Linfeng Cui,Yang'en You,Xueling Mi,Sanzhong Luo Org. Chem. Front. 2018 5 2313
• 4. A facile synthesis of 3,4-dimercaptofurans via sulfenylation of (E)-β-chlorovinyl ketones and 1,2-sulfur migration
  E. Song,H. Y. Kim,K. Oh Org. Biomol. Chem. 2017 15 1776
• 5. Synthesis of functionalized cyclopropylboronic esters based on a 1,2-metallate rearrangement of cyclopropenylboronate
  Haruki Mizoguchi,Masaya Seriu,Akira Sakakura Chem. Commun. 2020 56 15545

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Isoindoles and derivatives Isoindolones
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Isoindoles and derivatives Isoindolines Isoindolones
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides

N-(Phenylthio)phthalimide (CAS No. 14204-27-4): Properties, Applications, and Market Insights

N-(Phenylthio)phthalimide (CAS No. 14204-27-4) is a specialized organic compound that has garnered significant attention in the chemical and pharmaceutical industries. This compound, also known as N-Phenylthiophthalimide, belongs to the class of phthalimide derivatives, which are widely recognized for their versatility in synthetic chemistry. The CAS number 14204-27-4 uniquely identifies this compound, ensuring precise identification in research and commercial applications.

The molecular structure of N-(Phenylthio)phthalimide features a phthalimide core linked to a phenylthio group, which imparts unique chemical properties. This combination makes it a valuable intermediate in the synthesis of more complex molecules. Researchers and manufacturers often seek N-(Phenylthio)phthalimide CAS 14204-27-4 for its role in producing agrochemicals, pharmaceuticals, and advanced materials. Its stability and reactivity under controlled conditions make it a preferred choice for various chemical transformations.

One of the most common applications of N-(Phenylthio)phthalimide is in the field of polymer chemistry. It serves as a key building block for creating high-performance polymers with enhanced thermal and mechanical properties. Additionally, its use in photoinitiators and crosslinking agents has been explored, particularly in the development of UV-curable coatings and adhesives. The demand for such materials has surged due to the growing emphasis on sustainable and eco-friendly technologies.

In the pharmaceutical sector, N-(Phenylthio)phthalimide 14204-27-4 is utilized as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its ability to participate in N-acylation reactions and other key transformations makes it indispensable in drug development. Recent studies have also highlighted its potential in anticancer drug research, where its derivatives exhibit promising biological activity. This has led to increased interest from biotech companies and academic researchers alike.

The market for N-(Phenylthio)phthalimide CAS No. 14204-27-4 is influenced by several factors, including advancements in green chemistry and the shift toward bio-based materials. As industries strive to reduce their environmental footprint, the demand for efficient and sustainable chemical intermediates like N-(Phenylthio)phthalimide is expected to rise. Furthermore, the compound's compatibility with flow chemistry and continuous manufacturing processes aligns with modern industrial trends.

From a regulatory perspective, N-(Phenylthio)phthalimide is generally regarded as safe for handling when proper precautions are followed. However, users are advised to consult safety data sheets (SDS) and adhere to good laboratory practices (GLP). The compound's stability under standard storage conditions ensures its longevity, making it a reliable choice for long-term projects.

In conclusion, N-(Phenylthio)phthalimide (CAS 14204-27-4) is a multifaceted compound with broad applications across multiple industries. Its unique chemical properties, coupled with its role in innovative research and industrial processes, underscore its importance in modern chemistry. As the demand for specialty chemicals continues to grow, N-(Phenylthio)phthalimide is poised to remain a critical component in the chemical landscape.

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